Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,600 recalls have been distributed to Arizona in the last 12 months.
Showing 21001–21020 of 52,339 recalls
Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...
The Issue: Affected lots were manufactured with the protective release liner in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail...
The Issue: Firm is recalling two lots of 2 lb. organic soybeans because they have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The firm has become aware that there is a likelihood that a missing snap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Through a customer complaint and and internal investigation it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levetiracetam Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert - the incorrect package insert...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyophilized Sermorelin w/ GHRP2 3 mg For injection Recalled by Innoveix...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyophilized Chorionic Gonadotropin 11 Recalled by Innoveix Pharmaceuticals...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROX LAT HUMERAL LOCK PLATE Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLS Brevius Stem Kinectiv Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CABLE-READY SHORT GTR and CABLE-READY LONG GTR Recalled by Zimmer Biomet,...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various fixation systems and accessories Recalled by Zimmer Biomet, Inc. Due...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramic Femoral Heads Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.